Literature DB >> 8076406

Macrocephaly, distinct craniofacial appearance and spastic paraplegia: an autosomal recessive subtype of complicated spastic paraplegia.

J P Fryns1, M Hellemans, H Van den Berghe.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 8076406     DOI： 10.1111/j.1399-0004.1994.tb04146.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  1 in total

1.  Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?

Authors:  K H Orstavik; P Strømme; J Ek; A Torvik; O H Skjeldal
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.